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237647

L−(+)-α-Phenylglycine

Name: <SC>L−</SC>(+)-α-Phenylglycine
Brand: ALDRICH

99%

Synonym(s):

(S)-(+)-2-Phenylglycine, S-(+)-α-Aminophenylacetic acid, L-2-Phenylglycine

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About This Item

Linear Formula:

C₆H₅CH(NH₂)CO₂H

CAS Number:

2935-35-5

Molecular Weight:

151.16

UNSPSC Code:

12352209

NACRES:

NA.22

PubChem Substance ID:

24854260

EC Number:

220-909-8

Beilstein/REAXYS Number:

2208675

MDL number:

MFCD00064403

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Properties

Quality Level

100

assay

99%

form

powder

optical activity

[α]20/D +155°, c = 1 in 1 M HCl

reaction suitability

reaction type: solution phase peptide synthesis

mp

>300 °C (lit.)

application(s)

peptide synthesis

SMILES string

N[C@H](C(O)=O)c1ccccc1

InChI

1S/C8H9NO2/c9-7(8(10)11)6-4-2-1-3-5-6/h1-5,7H,9H2,(H,10,11)/t7-/m0/s1

InChI key

ZGUNAGUHMKGQNY-ZETCQYMHSA-N

Description

Application

Chiral starting material.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Chiral recognition of α-amino acids by an optically active (2S,5S,8S,11S)-2,5,8,11-tetraethyl cyclen cobalt(III) complex.

Shohei Tashiro et al.

Inorganic chemistry, 50(1), 4-6 (2010-12-01)

The optically active cobalt(III) complex with chiral cyclen, (2S,5S,8S,11S)-2,5,8,11-tetraethyl-1,4,7,10-tetraazacyclododecane, preferentially binds to D-phenylglycine (D-Phg) or D-t-leucine (D-t-Leu) rather than L-Phg or L-t-Leu, respectively, with 20% de in dimethyl sulfoxide at 293 K. Comparative studies on the crystal structures of cobalt(III)

Syntheses and highly enantioselective fluorescent recognition of α-aminocarboxylic acid anions using chiral oxacalix[2]arene[2]bisbinaphthes.

Kuoxi Xu et al.

Chirality, 24(8), 646-651 (2012-05-24)

The triazine-based bisbinaphthyl crown ethers oxacalix[2]arene[2]bisbinaphthes R-1, R-2, R-3 and S-1, S-2, S-3 were synthesized. The interactions of these compounds with various α-aminocarboxylic acid anions were studied. The crown ethers were found to carry out highly enantioselective fluorescent recognition of

Conformational study of jet-cooled L-phenylglycine.

Hyung Min Kim et al.

The Journal of chemical physics, 128(18), 184313-184313 (2008-06-06)

We investigated the conformational structures of L-phenylglycine in the gas phase by photoionization and double resonance spectroscopy techniques as well as high-level ab initio calculations. The UV-UV and IR-UV double resonance spectroscopy suggested that there exists only one conformer that

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Global Trade Item Number

SKU	GTIN
237647-100G	04061838786227
237647-25G	04061838786234